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Open AccessJournal ArticleDOI

GPRC6A Null Mice Exhibit Osteopenia, Feminization and Metabolic Syndrome

TLDR
The overall function of GPRC6A may be to coordinate the anabolic responses of multiple tissues through the sensing of extracellular amino acids, osteocalcin and divalent cations.
Abstract
Background GPRC6A is a widely expressed orphan G-protein coupled receptor that senses extracellular amino acids, osteocalcin and divalent cations in vitro. The physiological functions of GPRC6A are unknown.

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Journal ArticleDOI

Endocrine regulation of male fertility by the skeleton

TL;DR: It is shown that, in males, bone acts as a regulator of fertility, and the physiological repertoire of osteocalcin is expanded, providing the first evidence that the skeleton is an endocrine regulator of reproduction.
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New insights into the biology of osteocalcin

TL;DR: It is suggested that the ability of osteocalcin to function both locally in bone and as a hormone depends on a novel post-translational mechanism that alters osteoccin's affinity for the bone matrix and bioavailability.
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Genome-wide association study identifies five new susceptibility loci for prostate cancer in the Japanese population

TL;DR: Five new loci for prostate cancer susceptibility are reported here, at 5p15 (λ-corrected probability PGC = 3.9 × 10−18), GPRC6A/RFX6 (PGC = 1.6 ×10−12), 13q22 ( PGC = 2.8 × 10–10−9), C2orf43 (PGD = 7.5 × 10.–8) and FOXP4 (PGE = 7−8).
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Paracrine and endocrine actions of bone—the functions of secretory proteins from osteoblasts, osteocytes, and osteoclasts

TL;DR: The recent progresses in the paracrine and endocrine functions of the secretory proteins of osteoblasts, osteocytes, and osteoclasts are reviewed, revealing connections of the skeleton with other tissues and providing added insights into the pathogenesis of degenerative diseases affecting multiple organs and the drug discovery process.
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Strontium signaling: molecular mechanisms and therapeutic implications in osteoporosis.

TL;DR: This review focuses on the more recent knowledge of strontium signaling in bone cells and describes how the resulting pharmacological actions on bone metabolism have important therapeutic implications in the treatment of age-related bone loss and possibly other disorders.
References
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Journal ArticleDOI

Endocrine Regulation of Energy Metabolism by the Skeleton

TL;DR: It is shown that mice lacking the protein tyrosine phosphatase OST-PTP are hypoglycemic and are protected from obesity and glucose intolerance because of an increase in beta-cell proliferation, insulin secretion, and insulin sensitivity, and in vivo osteocalcin can improve glucose tolerance.
Journal ArticleDOI

Osteocalcin differentially regulates β cell and adipocyte gene expression and affects the development of metabolic diseases in wild-type mice

TL;DR: It is shown that long-term treatment of WT mice with osteocalcin can significantly weaken the deleterious effect on body mass and glucose metabolism of gold thioglucose-induced hyperphagia and high-fat diet and suggest that osteocalin may be of value in the treatment of metabolic diseases.
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A PCR primer bank for quantitative gene expression analysis

TL;DR: An experimentally validated algorithm for the identification of transcript-specific PCR primers on a genomic scale that can be applied to real-time PCR with sequence-independent detection methods is presented.
Journal ArticleDOI

Osteoclast-derived activity in the coupling of bone formation to resorption

TL;DR: It is argued that osteoclasts contribute in important ways to the transiently activated osteoclast, and stimulate osteoblast lineage cells to begin replacing the resorbed bone in each BMU.
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